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日本系统性红斑狼疮患者的治疗模式和医疗费用:一项回顾性理赔数据库研究。

Treatment patterns and medical cost of systemic lupus erythematosus patients in Japan: a retrospective claims database study.

机构信息

Health Economics Department, Janssen Pharmaceutical K.K, Tokyo, Japan.

Department of Pharmacy Practice, Faculty of Pharmaceutical Sciences, Center of Pharmaceutical Outcomes Research, Naresuan University, Phitsanulok, Thailand.

出版信息

J Med Econ. 2020 Jul;23(7):786-799. doi: 10.1080/13696998.2020.1740236. Epub 2020 Mar 31.

Abstract

To describe the characteristics and medication treatment patterns, healthcare resource utilization (HRU), and associated costs in Japanese patients with systemic lupus erythematosus (SLE). Claims data from the Japan Medical Data Center (JMDC) database were used to identify patients with SLE-related claims from 2010 to 2017. Algorithms were developed to retrospectively categorize patients by disease severity, treatment experience, and SLE-related manifestations such as lupus nephritis and central nervous system lupus. Descriptive and multivariate analyses were used to describe treatment pattern and estimate HRU and associated costs for the SLE cohort overall and by disease severity and complications. Among 4,733 eligible patients, 2,072 (43.8%) were treatment naïve, 2,214 (46.8%) were previously treated for SLE, and 447 (9.4%) did not receive any treatment. Mean (SD) age of the total SLE cohort was 45.2 (13.1) years and mean (SD) follow-up duration was 1,137.3 (758.0) d. Based on disease severity, 1,383 (29.2%) patients had mild, 2,619 (55.3%) patients had moderate, and 731 (15.4%) patients had severe SLE. Patients on glucocorticoids (both oral and parenteral) received add-on medications the most (35.5%,  < .001). Mean annual cost per SLE patient in the post-index period, inclusive of hospitalizations, outpatient visits, and pharmacy was ¥436,836; ¥1,010,772; and ¥2,136,780 for patients with mild, moderate, and severe SLE, respectively. The database only captured information on patients up to 75 years of age. Due to the nature of the database, biases regarding conditions that attribute to the spectrum of SLE severity, flare incidences, or individual physical status cannot be ruled out. This study describes the treatment patterns and economic burden experienced by Japanese patients with SLE. The results highlight an unmet need to derive better treatment strategies for patients with SLE to effectively address the disease burden in Japan.

摘要

描述日本系统性红斑狼疮(SLE)患者的特征、药物治疗模式、医疗资源利用(HRU)及相关费用。利用日本医药数据中心(JMDC)数据库中的理赔数据,从 2010 年至 2017 年确定与 SLE 相关的理赔患者。开发了算法以回顾性地根据疾病严重程度、治疗经验以及狼疮肾炎和中枢神经系统狼疮等 SLE 相关表现对患者进行分类。采用描述性和多变量分析描述 SLE 队列的治疗模式,并总体以及根据疾病严重程度和并发症估计 SLE 队列的 HRU 和相关费用。在 4733 名合格患者中,2072 名(43.8%)为治疗初治患者,2214 名(46.8%)为之前接受过 SLE 治疗的患者,447 名(9.4%)未接受任何治疗。SLE 总队列的平均(SD)年龄为 45.2(13.1)岁,平均(SD)随访时间为 1137.3(758.0)天。根据疾病严重程度,1383 名(29.2%)患者为轻度,2619 名(55.3%)患者为中度,731 名(15.4%)患者为重度 SLE。接受糖皮质激素(口服和静脉)治疗的患者接受附加药物治疗的比例最高(35.5%,<0.001)。索引后期间每位 SLE 患者的年平均费用,包括住院、门诊和药房费用分别为 436836 日元、1010772 日元和 2136780 日元,轻度、中度和重度 SLE 患者分别为 436836 日元、1010772 日元和 2136780 日元。该数据库仅捕获了 75 岁以下患者的信息。由于数据库的性质,无法排除导致 SLE 严重程度谱、发作发生率或个体身体状况的条件相关的偏倚。本研究描述了日本 SLE 患者的治疗模式和经济负担。结果强调需要制定更好的 SLE 患者治疗策略,以有效应对日本的疾病负担。

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